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Bupivacaine Hydrochloride
Bupivacaine Hydrochloride - 0409-5757-01 - (BUPIVACAINE HYDROCHLORIDE)
Drug Information of Bupivacaine Hydrochloride
| Product NDC: | 0409-5757 |
| Proprietary Name: | Bupivacaine Hydrochloride |
| Non Proprietary Name: | BUPIVACAINE HYDROCHLORIDE |
| Active Ingredient(s): | 5 mg/mL & nbsp; BUPIVACAINE HYDROCHLORIDE |
| Administration Route(s): | EPIDURAL; INFILTRATION; INTRACAUDAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bupivacaine Hydrochloride
| Product NDC: | 0409-5757 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018053 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100519 |
Package Information of Bupivacaine Hydrochloride
| Package NDC: | 0409-5757-01 |
| Package Description: | 200 AMPULE in 1 CASE (0409-5757-01) > 20 mL in 1 AMPULE |
NDC Information of Bupivacaine Hydrochloride
| NDC Code | 0409-5757-01 |
| Proprietary Name | Bupivacaine Hydrochloride |
| Package Description | 200 AMPULE in 1 CASE (0409-5757-01) > 20 mL in 1 AMPULE |
| Product NDC | 0409-5757 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BUPIVACAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; INFILTRATION; INTRACAUDAL |
| Start Marketing Date | 20100519 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | BUPIVACAINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Local Anesthesia [PE] |
